Abstract

Systemic sclerosis is usually considered to be the main cause of cutaneous sclerosis, but many other diseases can also manifest as cutaneous sclerosis and tissue fibrosis in clinic, which are easy to be confused with systemic sclerosis. This kind of diseases include a wide spectrum of heterogeneous diseases, ranging from a benign disease with a localized cutaneous involvement, to a widespread systemic, life-threatening disease. This review summarizes several main kinds of cutaneous fibrosing disorders, such as nephrogenic fibrosing dermopathy, scleromyxedema, POEMS syndrome, myeloma, Buschke scleroderma, eosinophilic fasciitis, eosinophilia-myalgia syndrome, carcinoid syndrome, porphyria cutanea tarda, chronic graft-versus host disease, environmentally triggered scleroderma-like disorders. Distinguishing the pathogenesis, clinical and pathological manifestations and therapeutic methods between this group of diseases will improve the understanding of these diseases, and has great clinical significance for their correct diagnosis and proper treatment. Key words: Scleroderma, systemic; Patient simulation; Pathology; Diagnosis; Therapeutic uses

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call